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Kauffmann olefination : ウィキペディア英語版 | Kauffmann olefination The Kauffmann olefination is a chemical reaction to convert aldehydes and ketones to olefins with a terminal methylene group. This reaction was discovered by the German chemist Thomas Kauffmann and is related to the better known Tebbe olefination or Wittig reaction. == Formation of the reagent == The reagent was generated ''in situ'' by conversion of different halogenides of molybdenum or tungsten with methyllithium at low temperatures (−78 °C). During the warm-up process the formation of the active reagent occurs. nmr-experiments has shown that the active reagent is not a Schrock carbene (e.g. Tebbe-reagent).
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